BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    I.V. CATHETER PLACEMENT UNIT

    K Number: K770181 · Decision Mar 30, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    10
    Review Days
    62

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    Basic Information

    Device Name
    I.V. CATHETER PLACEMENT UNIT
    K Number
    K770181
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    American Viggo
    Date Received
    January 27, 1977
    Decision Date
    March 30, 1977
    Product Code
    FOZ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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    Other Clearances by American Viggo

    K Number Device Name
    K771339 MALE LUER LOCK PLUG
    K770528 NEEDLE, MEMBRANE
    K770174 LUER-LOCK EXTENSION SET
    K770154 3-WAY STOPCOCK WITH LUER-LOCK FITTING
    K770096 EPIDURAL BLOCK PROCEDURE PACK
    K760666 4-WAY STOPCOCK W/LUER-LOCK FITTING
    K760679 4-WAY STOPCOCK W/7CM TUBING,
    K760678 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK
    K760667 4-WAY STOPCOCK W/10 CM EXTEN. TUBING